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nasty-shy [4]
3 years ago
15

PLEASE HELP ASAP !!

Chemistry
1 answer:
Ivenika [448]3 years ago
8 0

Answer:

  • 2SO₂ +  O₂ + 2H₂O  -----------> 2H₂SO₄
  • Theoretical yield of H₂SO₄ = 213 g
  • percent yield of H₂SO₄ = 94 %  

Explanation:

Data Given:

volume of SO₂ = 48.6 L

mass of H₂SO₄ = 200 g

balance equation = ?

theoretical yield = ?

percent yield = ?

Solution:

Part 1:

first we have to write a balance equation for the reaction

SO₂ gas react with water (H₂O) and excess oxygen

The balanced equation is as under

                       2SO₂ +  O₂ + 2H₂O  -----------> 2H₂SO₄

Part 2:

Now we have to find theoretical yield

First look at the balance reaction

                        2SO₂ +  O₂ + 2H₂O  -----------> 2H₂SO₄

                        2 mol                                         2 mol

2 moles of SO₂ give gives 2 moles of H₂SO₄

Now calculate volume of 2 moles of SO₂ and mass of 2 moles of H₂SO₄

volume of 2 moles of SO₂

Formula used

                 volume of gas = no. of moles x molar volume . . . . . . (1)

molar volume of SO₂= 22.4 L/mol

Put values in above formula (1)

                 volume of gas = 2 mol x 22.4 L/mol

                 volume of gas = 44.8 L

volume of 2 mole of SO₂ = 44.8 L

Now,

Find mass of 2 mole H₂SO₄

Formula Used

            mass in grams = no. of moles x molar mass . . . . . . . (2)

molar mass of H₂SO₄ = 2 (1) + 32 + 4(16)

molar mass of H₂SO₄ = 98 g/mol

put values in equation 2

        mass in grams = 2 mol x 98 g/mol

        mass in grams = 196 g

mass of 2 mole of H₂SO₄ = 196 g

** So,

Now we come to know that

44.8 L of SO₂ gives 196 g of H₂SO₄ then how many grams of the H₂SO₄ will be produced by 48.6 L of SO₂

Apply unity Formula

               44.8 L of SO₂ ≅ 196 g of H₂SO₄

               48.6 L of SO₂ ≅ X g of H₂SO₄

Do cross multiplication

                g of H₂SO₄  = 196 g x 48.6 L / 44.8 L

                g of H₂SO₄  =  213 g

So that is why the theoretical yield of H₂SO₄ is 213 g

Theoretical yield of H₂SO₄ = 213 g

Part 3

Calculate Percent Yield:

Formula used for this purpose:

             percent yield = actual yield /theoretical yield x 100 %

Put value in the above formula

           percent yield = 200 g/ 213 g x 100 %

          percent yield = 94 %    

So percent yield of H₂SO₄ = 94 %    

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The molar entropy of the evaporation of Trichlorofluoromethan :

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The molar entropy of the evaporation of Trichlorofluoromethan is 83.516 J/molK.

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b) 1.87

Explanation:

At the onset of the equivalence point (i.e the first equivalence point); alaninate is being converted to alanine.

H_2NC_2H_5CO^-_2  +  H^+  ------>  H_3}^+NC_2H_5CO^-_2

1 mole of  alaninate react with 1 mole of acid to give 1 mole of alanine;

therefore 50.0 mL  of 0.160 M alaninate required 50.0 mL of 0.160M HCl to reach the first equivalence point.

The concentration of alanine can be gotten via  the following process as shown below;

[H_3}^+NC_2H_5CO^-_2] = \frac{initial moles of alaninate}{total volume}

[H_3}^+NC_2H_5CO^-_2] = \frac{(50.0mL)*(0.160M)}{(50.0mL+50.0mL)}

[H_3}^+NC_2H_5CO^-_2] = \frac{8}{100mL}

[H_3}^+NC_2H_5CO^-_2] = 0.08 M

Alanine serves as an intermediary form, however the concentration of H^+ and the pH can be determined as follows;

[H^+] = \sqrt{\frac{K_{a1}K_{a2}{[H_3}^+NC_2H_5CO^-_2]+K_{a1}K_w}{  K_{a1}{[H_3}^+NC_2H_5CO^-_2]  } }

[H^+] = \sqrt{\frac{ (10^{-pK_{a1})}(10^{-pK_{a2})}(0.08)+(10^{-pK_{a1})}(1.0*10^{-14})}  {(10^{-pK_{a1}})+(0.08)} }

[H^+] = \sqrt{\frac{ (10^{-2.344})(10^{-9.868})(0.08)+(10^{-2.344})(1.0*10^{-14})}  {(10^{-2.344})+(0.08)} }

[H^+] =  7.63*10^{-7}M

pH = - log [H^+]

pH = -log[7.63*10^{-7}]

pH= 6.12

Therefore, the pH of the first equivalent point = 6.12

b) At the second equivalence point; all alaninate is converted into protonated alanine.

H_2NC_2H_5CO^-_2    +  H^+     ----->   H^+_3NC_2H_5CO^-_2

H^+_3NC_2H_5CO^-_2    +  H^+     ----->   H^+_3NC_2H_5CO_2H

Here; we have a situation where 1 mole of alaninate react with 2 moles of acid to give 1 mole of protonated alanine;

Moreover, 50.0 mL of 0.160 M alaninate is needed to produce 100.0mL of 0.160 M HCl in order to achieve the second equivalence point.

Thus, the concentration of protonated alanine can be determined as:

[H^+_3NC_2H_5CO_2H] = \frac{initial moles of alaninate}{total volume}

[H^+_3NC_2H_5CO_2H] = \frac{(50.0mL)*(0.160M)}{(50.0mL+100.0mL)}

[H^+_3NC_2H_5CO_2H] = \frac{8}{150}

[H^+_3NC_2H_5CO_2H] = 0.053 M

The pH at the second equivalence point can be calculated via the dissociation of protonated alanine at equilibrium which is represented as:

H^+_3NC_2H_5CO_2H        ⇄        H^+_3NC_2H_5CO^-_2    +  H^+

(0.053 - x)                                  x                             x

K_{a1} = \frac{[H^+] [H^+_3NC_2H_5CO^-_2]}{[H^+_3NC_2H_5CO_2H]}

10^{-PK_{a1}} = \frac{x*x}{(0.053-x)}

10^{-2.344} =\frac{x^2}{(0.053-x)}

0.00453 = \frac{x^2}{(0.053-x)}

0.00453(0.053-x) =x^2

x^2+0.00453x-(2.4009*10^{-4})

Using quadratic equation formula;

\frac{-b+/-\sqrt{b^2-4ac} }{2a}

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\frac{-0.00453+\sqrt{(0.00453)^2-4(1)(-2.4009*10^{-4})} }{2(1)} OR \frac{-0.00453-\sqrt{(0.00453)^2-4(1)(-2.4009*10^{-4})} }{2(1)}

= 0.0134                    OR                -0.0179

So; we go by the positive integer which says

x = 0.0134

So [H^+]=[H_3^+NC_2H_5CO^-_2]= 0.0134 M

pH = -log[H^+]

pH = -log[0.0134]

pH = 1.87

Thus, the pH of the second equivalent point = 1.87

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